🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Dina Ahram

Quest Diagnostics (United Kingdom)

ORCID: 0000-0003-4617-3938

Also affiliated with Quest Diagnostics (United States)

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 8 papers. Top paper: “De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis”.

De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.01.008

N/A

1.2DataRank · unranked

27 citations

Amar J. Majmundar, Kamal Khan, Tze Yin Lim, Shirlee Shril, Gina Jin +62 more

Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome

Nature Communications(2023)10.1038/s41467-023-37985-w

N/A

1.1DataRank · unranked

51 citations

Michelle T. McNulty, Xiaoyuan Jia, Yask Gupta, Hanna Dêbiec, Yang Luo +65 more

Natural History and Clinicopathological Associations of TRPC6-Associated Podocytopathy

Journal of the American Society of Nephrology(2024)10.1681/asn.0000000501

N/A

0.709DataRank · unranked

16 citations

Andrew Beenken, Elena Martinelli, Ken Saida, Andrea L. Knob, Juntao Ke +45 more

Implementation and Feasibility of Clinical Genome Sequencing Embedded Into the Outpatient Nephrology Care for Patients With Proteinuric Kidney Disease

Kidney International Reports(2023)10.1016/j.ekir.2023.05.021

N/A

0.241DataRank · unranked

4 citations

Dina Ahram, Atteeq U. Rehman, Adele Mitrotti, Avinash Abhyankar, Namrata G. Jain +20 more

Clinical Real-Time Genome Sequencing to Solve the Complex and Confounded Presentation of a Child With Focal Segmental Glomerulosclerosis and Multiple Malignancies

Kidney International Reports(2022)10.1016/j.ekir.2022.07.174

N/A

0DataRank · unranked

3 citations

Dina Ahram, Maddalena Marasà, Ateeq Ur Rehman, Halie May, Stergios Zacharoulis +11 more

Multidisciplinary approaches for elucidating genetics and molecular pathogenesis of urinary tract malformations

Kidney International(2021)10.1016/j.kint.2021.09.034

N/A

0DataRank · unranked

27 citations

Dina Ahram, Yangfan P. Liu, Rik Westland, Rosemary V. Sampogna, Nicholas Katsanis +3 more

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis

Journal of the American Society of Nephrology(2023)10.1681/asn.0000000000000132

N/A

0DataRank · unranked

15 citations

Tze Yin Lim, Juntao Ke, Gina Jin, Miguel Verbitsky, Monica Bodria +77 more

Pilot Study of Return of Genetic Results to Patients in Adult Nephrology

Clinical Journal of the American Society of Nephrology(2020)10.2215/cjn.12481019

N/A

0DataRank · unranked

47 citations

Maddalena Marasà, Hila Milo Rasouly, Emily Groopman, S. Ali Husain, Sumit Mohan +19 more